ClinVar Miner

List of variants in gene MRPS22 reported as pathogenic for Inborn genetic diseases

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_020191.4(MRPS22):c.373C>T (p.Arg125Ter)	rs780703525	0.00001
NM_020191.4(MRPS22):c.489T>G (p.Tyr163Ter)	rs201337850	0.00001

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